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Sample GSM754675 Query DataSets for GSM754675
Status Public on Jul 05, 2012
Title E. coli O157:H7 EDL933 in LB at 37oC for 7 hrs incubation with DMSO
Sample type RNA
 
Source name RNA extracted from e. coli o157: H7 EDL933 cells grown (7 hrs incubation) in LB at 37ºC with DMSO
Organism Escherichia coli
Characteristics serotype: O157:H7
strain: EDL933
Extracted molecule total RNA
Extraction protocol E. coli O157:H7 EDL933 was inoculated in 100 ml of LB in 250 ml shake flasks with overnight cultures that were diluted 1:100. Cells were shaken with 4 g of glass wool at 250 rpm and 37°C for 7 hrs. Cells were immediately chilled with dry ice and 95% ethanol (to prevent RNA degradation) for 30 sec before centrifugation in 50 ml centrifuge tubes at 13,000 g for 2 min; cell pellets were frozen immediately with dry ice and stored -80°C. RNA was isolated using Qiagen RNeasy mini Kit (Cat# 74104) with Qiagen RNase-free DNase I (Cat# 79254).
Label biotin
Label protocol Following affymetrix protocol.
cDNA was synthesized first using Promega M-MLV Reverse transcriptase (cat# M1705). After removing RNA, DNA fragmentation was performed to obtain and 50-200 base cDNA fragments. The fragmented cDNA was labelled with Biotin-ddUTP using Enzo BioArray Terminal Labeling Kit (Affymetrix, P/N 900181).
 
Hybridization protocol Following affymetrix protocol.
Prepared hybridization cocktail for Single Probe Array (49 Format) with total 200 ul volume including 1X hybrization buffer, 50 pM B2 Control Oligo, 0.1 mg/mL Herring Sperm DNA, 0.5 mg/mL BSA, and at least 1 ug fragmented and labelled cDNA.
After loading of hybridization cocktail in Affymetrix E. coli Antisense Genome Array, the hybridization was performed at 45ºC, with 60 rpm for 16 hours.
After hybridization, the probe array was washed and stained using Affymetrix Genechip Fluidics Station 450 and the software GenomeChipOperating Software (GCOS).
Scan protocol Following affymetrix protocol.
After washing and staining, the probe array was scanned using Affymetrix Genechip scanner GCS3000 7G system and the software GenomeChipOperating Software (GCOS).
Description RNA extracted from E. coli EDL933 cells grown on glass wool for 7 hrs in LB at 37ºC
Data processing MAS 5.0 Expression Analysis Default Setting
 
Submission date Jul 06, 2011
Last update date Jul 05, 2012
Contact name Jintae Lee
E-mail(s) jtlee@ynu.ac.kr
Phone 82-53-810-2533
Organization name Yeungnam University
Department Chemical engineering
Lab Biotechnology
Street address 214-1 Daedong
City Gyeongsan-Si
State/province Gyeongsangbuk-Do
ZIP/Postal code 712-749
Country South Korea
 
Platform ID GPL3154
Series (1)
GSE30424 Indole-3-Acetaldehyde Inhibits Escherichia coli O157:H7 Biofilm Formation by Reducing Curli Formation

Data table header descriptions
ID_REF
VALUE Signal intensity accepted from the probeset
ABS_CALL Probeset signal: absent or present
DETECTION P-VALUE Probeset signal: p-value (shows the coherency of the results)

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 66.9688 P 0.0103112
AFFX-BioB-M_at 86.2323 P 0.000581214
AFFX-BioB-3_at 54.5345 A 0.52976
AFFX-BioC-5_at 19.2965 A 0.275076
AFFX-BioC-3_at 33.7984 A 0.116031
AFFX-BioDn-5_at 11.6854 A 0.411357
AFFX-BioDn-3_at 39.0481 A 0.205692
AFFX-CreX-5_at 0.836218 A 0.963468
AFFX-CreX-3_at 1.87779 A 0.999421
AFFX-DapX-5_at 10115.7 P 4.42873e-05
AFFX-DapX-M_at 6251.28 P 4.42873e-05
AFFX-DapX-3_at 5183.12 P 4.42873e-05
AFFX-LysX-5_at 557.506 P 0.000146581
AFFX-LysX-M_at 252.683 P 0.000296708
AFFX-LysX-3_at 160.636 P 0.000968611
AFFX-PheX-5_at 965.856 P 4.42873e-05
AFFX-PheX-M_at 602.195 P 9.4384e-05
AFFX-PheX-3_at 548.157 P 0.000146581
AFFX-ThrX-5_at 1908.63 P 4.42873e-05
AFFX-ThrX-M_at 2123.75 P 0.000146581

Total number of rows: 10208

Table truncated, full table size 323 Kbytes.




Supplementary file Size Download File type/resource
GSM754675.CEL.gz 754.3 Kb (ftp)(http) CEL
GSM754675.CHP.gz 113.0 Kb (ftp)(http) CHP
Processed data included within Sample table
Processed data provided as supplementary file
Processed data are available on Series record

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